6365 - Senior CQV Engineer / Senior Validation Engineer

Verista; Harvard (MA); On-site; USD 70,491 - 118,062; Full time

Benefits offered by this job

Medical, Dental & Vision insurances

401(k) Retirement Plan

Paid Time Off and Holidays

Tuition Reimbursement

Job summary

Verista is looking for a Senior Validation Engineer to join their team in Devens, MA. This role involves executing IQ/OQ protocols, performing equipment and drawing verifications, and supporting temperature mapping activities. Ideal candidates have 3–8 years of CQV/validation experience and a Bachelor's degree in a relevant STEM field.

The role offers competitive pay, performance-based incentives, and comprehensive benefits including medical, dental, and 401(k) plans. Join Verista's mission to empower growth in the life sciences industry!

Qualifications

• 3–8 years of experience in CQV/validation.
• Hands-on experience with bioprocess equipment preferred.
• Exposure to temperature mapping is a plus.

Responsibilities

• Execute IQ/OQ protocols and support operational verification activities.
• Perform drawing walkdowns and equipment verification.
• Identify and document deviations in compliance with GMP/GDP.

Skills

CQV/validation experience

GMP/GDP fundamentals

Process equipment validation

IQ/OQ execution

Field verification activities

Education

Bachelor’s Degree in STEM

Tools

eVal

ValGenesis

Temperature mapping tools

Job description

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision‑making and are the result of our significant investment in our people and our capabilities.

Senior Validation Engineer Responsibilities

• Execute IQ/OQ protocols and support operational verification activities
• Perform drawing walkdowns (P&IDs, system verification)
• Perform equipment/component verification
• Perform MOC and weld verification
• Support temperature mapping activities using data loggers and validation tools
• Assist with SIP/CIP execution and cycle development activities
• Identify and document deviations and support investigations
• Ensure accurate and complete documentation in compliance with GMP/GDP standards
• Work collaboratively with engineering, QA, and operations teams

Job Requirements

• Bachelor’s Degree or equivalent required (STEM degree, Biomedical Engineering, Chemical Engineering preferred)
• 3–8 years of CQV/validation experience
• Hands‑on experience executing validation for process equipment
• Strong GMP/GDP fundamentals
• Experience with IQ/OQ execution and field verification activities
• Experience with eVal (required), ValGenesis a plus
• Exposure to temperature mapping (Ellab a plus)
• Experience with bioprocess equipment preferred (bioreactors, filtration, chromatography, UF)

This role requires the ability to be on‑site, full‑time in Devens, MA.

National (US) Range: $70,491 USD - $118,062 USD

Benefits

• High growth potential and fast‑paced organization with a people‑focused culture
• Competitive pay plus performance‑based incentive programs
• Company‑paid Life, Short‑Term, and Long‑Term Disability Insurance
• Medical, Dental & Vision insurances
• FSA, DCARE, Commuter Benefits
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 401(k) Retirement Plan (Employer Matching benefit)
• Paid Time Off (Rollover Option) and Holidays
• As Needed Sick Time
• Tuition Reimbursement
• Team Social Activities
• Employee Recognition
• Employee Referral Program
• Paid Parental Leave and Bereavement

Verista is an equal opportunity employer.